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Mon Aug 28 12:14:28 2006

A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
James C, Ugo V, Le Couedic JP, Staerk J, et al.
NATURE 434 (7037): 1144-1148, APR 28 2005
and the citing papers
Nodes: 181, Authors: 753, Journals: 66, Cited References: 5591, Words: 617
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Collection span: 2005 - 2006
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#LCRNCRNode / Date / Journal / AuthorLCSGCS
102743 2005 NATURE 434 (7037): 1144-1148
James C; Ugo V; Le Couedic JP; Staerk J; Delhommeau F; et al.
A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera
180180
21484 2005 BLOOD 106 (6): 2162-2168
Jones AV; Kreil S; Zoi K; Waghorn K; Curtis C; et al.
Widespread occurrence of the JAK2 V617F mutation in chronic myeloproliferative disorders
4856
313227 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280 (24): 22788-22792
Zhao RX; Xing S; Li Z; Fu XQ; Li QS; et al.
Identification of an acquired JAK2 mutation in Polycythemia vera
5256
4112345 2005 NEW ENGLAND JOURNAL OF MEDICINE 353 (2): 172-187
Krause DS; Van Etten RA
Tyrosine kinases as targets for cancer therapy
354
52189 2005 BLOOD 106 (10): 3370-3373
Jelinek J; Oki Y; Gharibyan V; Bueso-Ramos C; Prchal JT; et al.
JAK2 mutation 1849G > T is rare in acute leukemias but can be found in CMML, Philadelphia chromosome-negative CML, and megakaryocytic leukemia
2328
61236 2005 BLOOD 106 (8): 2862-2864
Goerttler PS; Steimle C; Marz E; Johansson PL; Andreasson B; et al.
The Jak2V617F mutation, PRV-1 overexpression, and EEC formation define a similar cohort of MPD patients
2326
723016 2005 BRITISH JOURNAL OF HAEMATOLOGY 131 (2): 208-213
Wolanskyj AP; Lasho TL; Schwager SM; McClure RF; Wadleigh M; et al.
JAK2(V617F) mutation in essential thrombocythaemia: clinical associations and long-term prognostic relevance
2125
832934 2005 LANCET 366 (9501): 1945-1953
Campbell PJ; Scott LM; Buck G; Wheatley K; East CL; et al.
Definition of subtypes of essential thrombocythaemia and relation to polycythaemia vera based on JAK2 V617F mutation status: a prospective study
1825
9117540 2005 MAYO CLINIC PROCEEDINGS 80 (7): 947-958
Tefferi A; Gilliland DG
The JAK2(V617F) tyrosine kinase mutation in myeloproliferative disorders: Status report and immediate implications for disease classification and diagnosis
1724
1032211 2005 BLOOD 106 (10): 3377-3379
Levine RL; Loriaux M; Huntly BJP; Loh ML; Beran M; et al.
The JAK2V617F activating mutation occurs in chronic myelomonocytic leukemia and acute myeloid leukemia, but not in acute lymphoblastic leukemia or chronic lymphocytic leukemia
1723
#LCRNCRNode / Date / Journal / AuthorLCSGCS
111838 2005 LEUKEMIA 19 (10): 1847-1849
Antonioli E; Guglielmelli P; Pancrazzi A; Bogani C; Verrucci M; et al.
Clinical implications of the JAK2 V617F mutation in essential thrombocythemia
1517
1225217 2005 BRITISH JOURNAL OF HAEMATOLOGY 131 (3): 320-328
Tefferi A; Lasho TL; Schwager SM; Steensma DP; Mesa RA; et al.
The JAK2(V617F) tyrosine kinase mutation in myelofibrosis with myeloid metaplasia: lineage specificity and clinical correlates
1316
1322715 2005 BRITISH JOURNAL OF HAEMATOLOGY 131 (2): 166-171
Tefferi A; Sirhan S; Lasho TL; Schwager SM; Li CY; et al.
Concomitant neutrophil JAK2(V617F) mutation screening and PRV-1 expression analysis in myeloproliferative disorders and secondary polycythaemia
1315
14118932 2005 JOURNAL OF CLINICAL ONCOLOGY 23 (26): 6285-6295
Frohling S; Scholl C; Gilliland DG; Levine RL
Genetics of myeloid malignancies: Pathogenetic and clinical implications
314
1512110 2005 BLOOD 106 (10): 3374-3376
Kralovics R; Teo SS; Buser AS; Brutsche M; Tiedt R; et al.
Altered gene expression in myeloproliferative disorders correlates with activation of signaling by the V617F mutation of Jak2
1011
1616128 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280 (29): 27251-27261
Royer Y; Staerk J; Costuleanu M; Courtoy PJ; Constantinescu SN
Janus kinases affect thrombopoietin receptor cell surface localization and stability
711
1724129 2005 JOURNAL OF BIOLOGICAL CHEMISTRY 280 (51): 41893-41899
Staerk J; Kallin A; Demoulin JB; Vainchenker W; Constantinescu SN
JAK1 and Tyk2 activation by the homologous polycythemia vera JAK2 V617F mutation - Cross-talk with IGF1 receptor
99
1823650 2005 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 102 (52): 18962-18967
Lu XH; Levine R; Tong W; Wernig G; Pikman Y; et al.
Expression of a homodimeric type I cytokine receptor is required for JAK2V617F-mediated transformation
99
1956960 2005 TRENDS IN MOLECULAR MEDICINE 11 (12): 546-554
James C; Ugo V; Casadevall N; Constantinescu SN; Vainchenker W
A JAK2 mutation in myeloproliferative disorders: pathogenesis and therapeutic and scientific prospects
89
201107 2005 BLOOD 106 (8): 2920-2921
Scott LM; Campbell PJ; Baxter EJ; Todd T; Stephens P; et al.
The V617F JAK2 mutation is uncommon in cancers and in myeloid malignancies other than the classic myeloproliferative disorders
88
#LCRNCRNode / Date / Journal / AuthorLCSGCS
2113621 2005 HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 90 (7): 871-874
Cazzola M; Skoda R
Gain of function, loss of control - A molecular basis for chronic myeloproliferative disorders
88
2218054 2005 SEMINARS IN HEMATOLOGY 42 (4): 230-238
Finazzi G; Harrison C
Essential thrombocythemia
68
2312348 2005 ONCOGENE 24 (48): 7248-7252
Bousquet M; Quelen C; De Mas V; Duchayne E; Roquefeuil B; et al.
The t(8;9)(p22;p24) translocation in atypical chronic myeloid leukaemia yields a new PCM1-JAK2 fusion gene
47
24219152 2005 SEMINARS IN HEMATOLOGY 42 (4): 206-220
Tefferi A; Spivak JL
Polycythemia vera: Scientific advances and current practice
67
251535 2005 LEUKEMIA 19 (9): 1692-1696
Murati A; Gelsi-Boyer V; Adelaide J; Perot C; Talmant P; et al.
PCM1-JAK2 fusion in myeloproliferative disorders and acute erythroid leukemia with t(8;9) translocation
46
2611544 2005 NEW ENGLAND JOURNAL OF MEDICINE 353 (1): 85-86
Barbui T; Finazzi G
When and how to treat essential thrombocythemia
26
2711918 2005 CANCER RESEARCH 65 (20): 9152-9154
Fitzgibbon J; Smith LL; Raghavan M; Smith ML; Debernardi S; et al.
Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias
05
28117822 2005 HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 90 (7): 949-968
Chalandon Y; Schwaller J
Targeting mutated protein tyrosine kinases and their signaling pathways in hematologic malignancies
05
29210830 2005 JOURNAL OF CLINICAL INVESTIGATION 115 (12): 3339-3347
Kaushansky K
The molecular mechanisms that control thrombopoiesis
15
30120033 2005 JOURNAL OF CLINICAL ONCOLOGY 23 (33): 8520-8530
Tefferi A
Pathogenesis of myelofibrosis with myeloid metaplasia
35
#LCRNCRNode / Date / Journal / AuthorLCSGCS
311546 2005 NEW ENGLAND JOURNAL OF MEDICINE 353 (13): 1416-1417
Tefferi A; Lasho TL; Gilliland G
JAK2 mutations in myeloproliferative disorders
45
3228141 2006 LEUKEMIA 20 (2): 350-353
James C; Delhommeau F; Marzac C; Teyssandier I; Le Couedic JP; et al.
Detection of JAK2 V617F as a first intention diagnostic test for erythrocytosis
45
335143151 2006 LEUKEMIA & LYMPHOMA 47 (2): 177-194
Nelson ME; Steensma DP
JAK2 V617F in myeloid disorders: What do we know now, and where are we headed?
35
341714 2005 BRITISH JOURNAL OF HAEMATOLOGY 130 (6): 968-968
Johan MF; Goodeve AC; Bowen DT; Frew ME; Reilly JT
JAK2 V617F Mutation is uncommon in chronic myelomonocytic leukaemia
34
3537825 2005 HEMATOLOGY 10: 215-223
Michiels JJ
Clinical, pathological and molecular features of the chronic myeloproliferative disorders: MPD 2005 and beyond
44
3617931 2005 JOURNAL OF CLINICAL INVESTIGATION 115 (12): 3370-3377
Macaulay IC; Carr P; Gusnanto A; Ouwehand WH; Fitzgerald D; et al.
Platelet genomics and proteomics in human heat and disease
04
3728156 2005 SEMINARS IN HEMATOLOGY 42 (4): 266-273
Skoda R; Prchal JT
Lessons from familial myeloproliferative disorders
44
3816680 2006 BLOOD 107 (1): 176-183
Lucet IS; Fantino E; Styles M; Bamert R; Patel O; et al.
The structural basis of Janus kinase 2 inhibition by a potent and specific pan-Janus kinase inhibitor
24
3953489 2006 BLOOD 107 (9): 3676-3682
Passamonti F; Rumi E; Pietra D; Della Porta MG; Boveri E; et al.
Relation between JAK2 (V617F) mutation status, granulocyte activation, and constitutive mobilization of CD34(+) cells into peripheral blood in myeloproliferative disorders
44
4052592 2006 BLOOD 107 (11): 4274-4281
Wernig G; Mercher T; Okabe R; Levine RL; Lee BH; et al.
Expression of Jak2V617F causes a polycythemia vera-like disease with associated myelofibrosis in a murine bone marrow transplant model
44
#LCRNCRNode / Date / Journal / AuthorLCSGCS
41769140 2006 LEUKEMIA 20 (2): 200-205
De Keersmaecker K; Cools J
Chronic myeloproliferative disorders: a tyrosine kinase tale
24
424181153 2006 LEUKEMIA & LYMPHOMA 47 (3): 381-396
Thiele J; Kvasnicka HM
A critical reappraisal of the WHO classification of the chronic myeloproliferative disorders
24
43115159 2006 ONCOGENE 25 (9): 1434-1436
Lee JW; Kim YG; Soung YH; Han KJ; Kim SY; et al.
The JAK2 V617F mutation in de novo acute myelogenous leukemias
44
441421 2005 AMERICAN JOURNAL OF PATHOLOGY 167 (3): 849-858
Vannucchi AM; Pancrazzi A; Guglielmelli P; Di Lollo S; Bogani C; et al.
Abnormalities of GATA-1 in megakaryocytes from patients with idiopathic myelofibrosis
33
451613 2005 BRITISH JOURNAL OF HAEMATOLOGY 130 (5): 800-801
Cario H; Goerttler PS; Steimle C; Levine RL; Pahl HL
The JAK2V617F mutation is acquired secondary to the predisposing alteration in familial polycythaemia vera
23
4618036 2005 LEUKEMIA 19 (10): 1739-1744
Delaval B; Lelievre H; Birnbaum D
Myeloproliferative disorders: the centrosome connection
13
47120841 2005 MAYO CLINIC PROCEEDINGS 80 (9): 1220-1232
Tefferi A; Barbui T
bcr/abl-negative, classic myeloproliferative disorders: Diagnosis and treatment
23
4823942 2005 MOLECULAR INTERVENTIONS 5 (4): 211-215
Pesu M; O'Shea J; Hennighausen L; Silvennoinen O
Identification of an acquired mutation in Jak2 provides molecular insights into the pathogenesis of myeloproliferative disorders
33
4938553 2005 SEMINARS IN HEMATOLOGY 42 (4): 221-229
Zhao ZJ; Vainchenker W; Krantz SB; Casadevall N; Constantinescu SN
Role of tyrosine kinases and phosphatases in Polycythemia vera
33
5027281 2006 BLOOD 107 (3): 907-915
Zhao W; Kitidis C; Fleming MD; Lodish HF; Ghaffari S
Erythropoietin stimulates phosphorylation and activation of GATA-1 via the PI3-kinase/AKT signaling pathway
03
#LCRNCRNode / Date / Journal / AuthorLCSGCS
512984 2006 BLOOD 107 (5): 2098-2100
Campbell PJ; Griesshammer M; Dohner K; Dohner H; Kusec R; et al.
V617F mutation in JAK2 is associated idiopathic myelofibrosis
33
52436122 2006 HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 91 (2): 169-175
Arellano-Rodrigo E; Alvarez-Larran A; Reverter JC; Villamor N; Colomer D; et al.
Increased platelet and leukocyte activation as contributing mechanisms for thrombosis in essential thrombocythemia and correlation with the JAK2 mutational status
33
5323185167 2006 SEMINARS IN THROMBOSIS AND HEMOSTASIS 32 (3): 174-207
Michiels JJ; Berneman Z; Van Bockstaele D; van der Planken M; De Raeve H; et al.
Clinical and laboratory features, pathobiology of platelet-mediated thrombosis and bleeding complications, and the molecular etiology of essential thrombocythemia and polycythemia vera: Therapeutic implications
33
541523 2005 ARCHIVES OF INTERNAL MEDICINE 165 (22): 2651-2658
Chim CS; Kwong YL; Lie AKW; Ma SK; Chan CC; et al.
Long-term outcome of 231 patients with essential thrombocythemia - Prognostic factors for thrombosis, bleeding, myelofibrosis, and leukemia
22
5531023 2005 HAEMATOLOGICA-THE HEMATOLOGY JOURNAL 90 (12): 1696-1697
McLornan DP; Percy MJ; Jones AV; Cross NCP; McMullin MF
Chronic neutrophilic leukemia with an associated V617F JAK2 tyrosine kinase mutation
22
561837 2005 LEUKEMIA 19 (10): 1843-1844
Tono C; Xu G; Toki T; Takahashi Y; Sasaki S; et al.
JAK2 Val617Phe activating tyrosine kinase mutation in juvenile myelomonocytic leukemia
22
5722851 2005 SEMINARS IN HEMATOLOGY 42 (4): 181-183
Skoda R; Prchal JT
Chronic myeloproliferative disorders - Introduction
22
58110455 2005 SEMINARS IN HEMATOLOGY 42 (4): 248-258
Barosi G; Hoffman R
Idiopathic myelofibrosis
22
5918661 2005 VIRCHOWS ARCHIV 447 (6): 909-919
Fend F; Bock O; Kremer M; Specht K; Quintanilla-Martinez L
Ancillary techniques in bone marrow pathology: molecular diagnostics on bone marrow trephine biopsies
12
60310379 2006 BIOCHEMICAL PHARMACOLOGY 71 (6): 713-721
Valentino L; Pierre J
JAW/STAT signal transduction: Regulators and implication in hematological malignancies
12
#LCRNCRNode / Date / Journal / AuthorLCSGCS
6142286 2006 BLOOD 107 (8): 3339-3341
Jones AV; Silver RT; Waghorn K; Curtis C; Kreil S; et al.
Minimal molecular response in polycythemia vera patients treated with imatinib or interferon alpha
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6251990 2006 BLOOD 107 (10): 4139-4141
Levine RL; Belisle C; Wadleigh M; Zahrieh D; Lee S; et al.
X-inactivation-based clonality analysis and quantitative JAK2V617F assessment reveal a strong association between clonality and JAK2V617F in PV but not ET/MMM, and identifies a subset of JAK2V617F-negative ET and NIMM patients with clonal hematopoiesis
22
63118134 2006 JOURNAL OF MOLECULAR DIAGNOSTICS 8 (2): 170-177
Bock O; Busche G; Koop C; Schroter S; Buhr T; et al.
Detection of the single hotspot mutation in the JH2 pseuclokinase domain of janus kinase 2 in bone marrow trephine biopsies derived from chronic myeloproliferative disorders
22
6459144 2006 LEUKEMIA 20 (4): 736-737
Bellosillo B; Besses C; Florensa L; Sole F; Serrano S
JAK2 V617F mutation, PRV-1 overexpression and endogenous erythroid colony formation show different coexpression patterns among Ph-negative chronic myeloproliferative disorders
22
6517152 2006 LEUKEMIA & LYMPHOMA 47 (2): 313-314
Lee JW; Soung YH; Kim SY; Nam SW; Park WS; et al.
JAK2 V617F mutation is uncommon in non-Hodgkin lymphomas
22
661734154 2006 LEUKEMIA RESEARCH 30 (6): 739-744
Tefferi A; Pardanani A
Mutation screening for JAK2(V617F): When to order the test and how to interpret the results
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67125160 2006 ONCOGENE 25 (18): 2679-2684
Weniger MA; Melzner I; Menz CK; Wegener S; Bucur AJ; et al.
Mutations of the tumor suppressor gene SOCS-1 in classical Hodgkin lymphoma are frequent and associated with nuclear phospho-STAT5 accumulation
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68139165 2006 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 103 (16): 6224-6229
Jamieson CHM; Gotlib J; Durocher JA; Chao MP; Mariappan MR; et al.
The JAK2 V617F mutation occurs in hematopoietic stem cells in polycythemia vera and predisposes toward erythroid differentiation
22
69122419 2005 CLINICAL AND LABORATORY HAEMATOLOGY 27 (3): 148-171
Bench AJ; Erber WN; Scott MA
Molecular genetic analysis of haematological malignancies: I. Acute leukaemias and myeloproliferative disorders
01
7016824 2005 HEMATOLOGICAL ONCOLOGY 23 (1): 26-33
Bowen DT
Chronic Myelomonocytic Leukemia: lost in classification?
01
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7119426 2005 INTERNATIONAL JOURNAL OF HEMATOLOGY 82 (2): 93-99
Choudhary C; Muller-Tidow C; Berdel WE; Serve H
Signal transduction of oncogenic Flt3
01
721847 2005 ONCOGENE 24 (48): 7125-7126
Mahon FX
JAK the trigger
01
7317849 2005 PATHOLOGY 37 (6): 479-492
Jack A
Organisation of neoplastic haematopathology services: a UK perspective
01
7416058 2005 SEMINARS IN ONCOLOGY 32 (4): 373-379
Martyre MC; Le Bousse-Kerdiles MC
Stem cell dysregulation in myelofibrosis with myeloid metaplasia: Current data on growth factor and transcription factor involvement
01
75122864 2006 AMERICAN JOURNAL OF CLINICAL PATHOLOGY 125 (4): 625-633
Murugesan G; Aboudola S; Szpurka H; Verbic MA; Maciejewski JP; et al.
Identification of the JAK2 V617F mutation in chronic myeloproliferative disorders using FRET probes and melting curve analysis
11
7616969 2006 ANNALS OF CLINICAL BIOCHEMISTRY 43: 97-104
Marsden JT
Erythropoietin - measurement and clinical applications
01
7792571 2006 ARCHIVES OF PATHOLOGY & LABORATORY MEDICINE 130 (7): 997-1003
Olsen RJ; Tang ZW; Farkas DH; Bernard DW; Zu YL; et al.
Detection of the JAK2(V617F) mutation in myeloproliferative disorders by melting curve analysis using the LightCycler system
11
7815285 2006 BLOOD 107 (6): 2219-2222
Burkitt MJ; Raafat A
Nitric oxide generation from hydroxyurea: significance and implications for leukemogenesis in the management of myeloproliferative disorders
01
7935288 2006 BLOOD 107 (9): 3495-3502
Zeuner A; Pedini F; Signore M; Ruscio G; Messina C; et al.
Increased death receptor resistance and FLIPshort expression in polycythemia vera erythroid precursor cells
11
803699 2006 BRITISH JOURNAL OF HAEMATOLOGY 132 (2): 244-245
Cheung B; Radia D; Pantelidis P; Yadegarfar G; Harrison C
The presence of the JAK2 V617F mutation is associated with a higher haemoglobin and increased risk of thrombosis in essential thrombocythaemia
01
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Targeting NF-kappa B in hematologic malignancies
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Hardee ME; Arcasoy MO; Blackwell KL; Kirkpatrick JP; Dewhirst MW
Erythropoietin biology in cancer
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Walz C; Sattler M
Novel targeted therapies to overcome imatinib mesylate resistance in chronic myeloid leukemia (CML)
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85186119 2006 GENETICS 172 (3): 1683-1697
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Mesa RA; Powell H; Lasho T; DeWald GW; McClure R; et al.
A longitudinal study of the JAK2(V617F) mutation in myelofibrosis with myelold metaplasia: analysis at two time points
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87422142 2006 LEUKEMIA 20 (3): 471-476
Quentmeier H; Macleod RAF; Zaborski M; Drexler HG
JAK2 V617F tyrosine kinase mutation in cell lines derived from myeloproliferative disorders
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88610143 2006 LEUKEMIA 20 (3): 534-535
Vizmanos JL; Ormazabal C; Larrayoz MJ; Cross NCP; Calasanz MJ
JAK2 V617F mutation in classic chronic myeloproliferative diseases: a report on a series of 349 patients
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Steensma DP; McClure RF; Karp JE; Tefferi A; Lasho TL; et al.
JAK2 V617F is a rare finding in de novo acute myeloid leukemia, but STAT3 activation is common and remains unexplained
11
901228146 2006 LEUKEMIA 20 (6): 1055-1060
Vannucchi AM; Pancrazzi A; Bogani C; Antonioli E; Guglielmelli P
A quantitative assay for JAK2(V617F) mutation in myeloproliferative disorders by ARMS-PCR and capillary electrophoresis
11
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91179156 2006 MOLECULAR AND CELLULAR BIOLOGY 26 (11): 4052-4062
Mazurkiewicz-Munoz AM; Argetsinger LS; Kouadio JLK; Stensballe A; Jensen ON; et al.
Phosphorylation of JAK2 at serine 523: a negative regulator of JAK2 that is stimulated by growth hormone and epidermal growth factor
01
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Yachimski PS; Chung RT; Sahani DV; Amrein PC; Misdraji J; et al.
A 46-year-old woman with sudden onset of abdominal distention - Budd-Chiari syndrome, with centrilobular hepatocellular necrosis, sinusoidal dilatation, congestion, and red-cell extravasation consistent with the presence of venous outflow obstruction. Heterozygosity for factor V Leiden. V617F mutation in JAK2.
01
939148169 2006 SEMINARS IN THROMBOSIS AND HEMOSTASIS 32 (3): 219-230
Thiele J; Kvasnicka HM
Clinicopathological criteria for differential diagnosis of thrombocythemias in various myeloproliferative disorders
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94235174 2006 SEMINARS IN THROMBOSIS AND HEMOSTASIS 32 (3): 283-288
Harrison CN
Management of essential thrombocythemia: Implications of the Medical Research Council Primary Thrombocythemia 1 trial
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95160181 2006 TRANSFUSION MEDICINE AND HEMOTHERAPY 33 (3): 217-226
Gnatenko DV; Bahou WF
Recent advances in platelet transcriptomics
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961332 2005 ARCHIVES DE PEDIATRIE 12 (8): 1249-1254
Mialou V; Kagialis-Girard S; Galambrun C; Pondarre C; Kebaili K; et al.
Thrombocytosis and essential thrombocytemia in childhood
00
97255 2005 BLOOD 106 (8): 2599-2599
Hoffman R
Let's not get too JAKed up!
00
98278 2005 BLOOD 106 (10): 3335-3336
Tefferi A
V617F "JAKs" up myeloproliferative signal
00
9927412 2005 BLOOD 106 (13): 4102-4113
Martelli F; Ghinassi B; Panetta B; Alfani E; Gatta V; et al.
Variegation of the phenotype induced by the Gatal(low) mutation in mice of different genetic backgrounds
00
10012920 2005 EXPERIMENTAL HEMATOLOGY 33 (11): 1299-1308
Corre-Buscail I; Pineau D; Boissinot M; Hermouet S
Erythropoietin-independent erythroid colony formation by bone marrow progenitors exposed to interleukin-11 and interleukin-8
00

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